# K193045: geko™ W-2

- Pathway: 510(k) (Special)
- Applicant: Firstkind Limited
- Decided: Jan 18, 2020 after 78 days
- Product code: IPF (Stimulator, Muscle, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K872976 (1987). 8 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180082: geko T-2 and geko Plus R-2, Firstkind, Ltd. (2018) Summary page 4.

## Most influential descendants
- K212762: geko W-2 (2021), 0 descendants of its own

## Indications for use
- Increasing local blood circulation - Edema reduction

Source page: https://510kreport.com/device/K193045
Methodology: https://510kreport.com/methodology